| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58326870-58327055 | Common:1; Rare:43 | ||||
| chr19:58327234-58327336 | Rare:25 | ||||
| chr19:58347566-58347792 | Common:8; Rare:106 | ||||
| chr19:58386734-58386831 | Common:3; Rare:31 | ||||
| chr19:58393141-58393426 | Common:3; Rare:68 | ||||
| chr19:58408449-58408777 | Common:4; Rare:101 | ||||
| chr19:58499206-58499545 | Common:2; Rare:111; Clinvar:4; Clinvar (benign):1 | ||||
| chr19:58547505-58547613 | Rare:41 | ||||
| chr19:58558908-58559145 | Common:1; Rare:73 | ||||
| chr19:58573316-58573503 | Rare:47 | ||||
| chr2:677358-677549 | Common:1; Rare:82 | ||||
| chr2:3377696-3377930 | Rare:68 | ||||
| chr2:3519381-3519622 | Common:2; Rare:77 | ||||
| chr2:3558251-3558695 | Common:6; Rare:163 | ||||
| chr2:3575095-3575384 | Common:2; Rare:85; Clinvar:3; Clinvar (benign):6 |